Novex™ Tris-Glycin SDS-Laufpuffer (10X)
Invitrogen™

Novex™ Tris-Glycin SDS-Laufpuffer (10X)

Novex Tris-Glycin SDS-Laufpuffer (10X) dient zum Trennen von Proteinen in ihrem denaturierten Zustand auf Tris-Glycin-Gelen. TRIS-Glycin-Gele ermöglichen die reproduzierbare TrennungWeitere Informationen
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KatalognummerMenge
LC2675500 ml
LC267544 x 1 l
LC267555 l
Katalognummer LC2675
Preis (EUR)
55,65
Exklusiv online
59,00
Ersparnis 3,35 (6%)
Each
Menge:
500 ml
Preis (EUR)
55,65
Exklusiv online
59,00
Ersparnis 3,35 (6%)
Each
Novex Tris-Glycin SDS-Laufpuffer (10X) dient zum Trennen von Proteinen in ihrem denaturierten Zustand auf Tris-Glycin-Gelen. TRIS-Glycin-Gele ermöglichen die reproduzierbare Trennung einer Vielzahl von Proteinen in gut aufgelöste Banden.

Native oder denaturierte Proteine trennen
Novex TRIS-Glycin-Gele enthalten kein SDS und können verwendet werden, um native und denaturierte Proteine genau zu trennen, je nach Probe und verwendeten Laufpuffern. Zum Trennen denaturierter Proteine auf Novex TRIS-Glycin-Gelen sollten Novex TRIS-Glycin-SD-Probenpuffer und Novex TRIS-Glycin-SD-Laufpuffer verwendet werden. Zur Trennung von nativen Proteinen verwenden Sie den nativen Novex TRIS-Glycin-Probenpuffer und den nativen Novex TRIS-Glycin-Laufpuffer.

Alle verfügbaren Puffer und Reagenzien für SDS-PAGE anzeigen

Nur für Forschungszwecke. Darf nicht für diagnostische Verfahren eingesetzt werden.
Specifications
Chemischer Name oder MaterialLaufpuffer
Empfohlene LagerungEnthält: Novex™ TRIS-Glycin-SD-Laufpuffer (10X), 500 ml
Lagerung: Bei +4 bis 25 °C lagern

Garantiert 6 Monate stabil, sofern in der Produktdokumentation nicht anders angegeben.
Konzentration10 X
Physikalische FormFlüssigkeit
ProduktlinieNovex
Menge500 ml
Unit SizeEach

Häufig gestellte Fragen (FAQ)

Where do I find buffer recipes for your precast protein gels?

The formulations of buffers for our precast protein gels can be found at this link: https://www.thermofisher.com/us/en/home/life-science/protein-biology/protein-gel-electrophoresis/protein-electrophoresis-buffers-reagents.html

Find additional tips, troubleshooting help, and resources within our Protein Electrophoresis and Western Blotting Support Center.

If a Tricine gel is accidentally run with buffers used in the Tris-Glycine system, what will happen and why?

If the Tricine gel is run with Tris-Glycine sample buffer, the bands will behave abnormally and resolve poorly. If the Tricine gel is accidentally run with Tris-Glycine running buffer, the gel will take longer to run and the resolution, especially for smaller proteins, will be worse than when the proteins are run on a Tris-Glycine gel with Tris-Glycine buffers. This is due to a combination of increase in stack area size (glycine is a slower ion than Tricine) and the higher ionic strength of the Tricine gel.

Find additional tips, troubleshooting help, and resources within our Protein Electrophoresis and Western Blotting Support Center.

How should I store Novex Tris-Glycine SDS Running Buffer (10X)?

We recommend storing Novex Tris-Glycine SDS Running Buffer (10X) at 4 to 25 degrees C.

Find additional tips, troubleshooting help, and resources within our Protein Electrophoresis and Western Blotting Support Center.

What are the recommended sample loading volumes and protein loading amounts for your precast protein gels?

*Tris-Glycine and Invitrogen Tricine Mini gels: see here (http://tools.thermofisher.com/content/sfs/manuals/electrophoresisguide_man.pdf), Page 8

*NuPAGE Tris-Acetate and NuPAGE Bis-Tris Mini gels: see here (http://tools.thermofisher.com/content/sfs/manuals/nupage_tech_man.pdf), Page 10

*Bolt Bis-Tris Plus Mini gels: see here (http://www.thermofisher.com/us/en/home/life-science/protein-biology/protein-gel-electrophoresis/protein-gels/bolt-bis-tris-gels.html)

*Thermo Scientific Precise Tris-HEPES gels: see here (https://tools.thermofisher.com/content/sfs/manuals/MAN0011499_Precise_Protein_Gels_UG.pdf), Page 1

*Midi gels (Invitrogen Tris-Glycine, NuPAGE Bis-Tris and NuPAGE Tris-Acetate): see here (https://assets.thermofisher.com/TFS-Assets/LSG/manuals/novex_midigel_man.pdf), Page 4

*Thermo Scientific Precise Tris-Glycine gels: see here (https://tools.thermofisher.com/content/sfs/manuals/D25MAN0011814_Precise_TrisGlycine_Gels_UG.pdf), Page 1

Find additional tips, troubleshooting help, and resources within our Protein Electrophoresis and Western Blotting Support Center.

Do your precast protein gels contain SDS?

Our precast protein gels do not contain SDS but they can be run under denaturing conditions when used with the appropriate denaturing running buffer.
Note: NuPAGE Bis-Tris gels, Bolt Bis-Tris Plus gels, and Thermo Scientific Precise Tris-HEPES gels cannot be run under native conditions; they can only be run under denaturing conditions.

*Invitrogen Tris-Glycine gels: For Native electrophoresis, use Invitrogen Tris-Glycine Native Running Buffer. For Denaturing electrophoresis, use Invitrogen Tris-Glycine SDS Running Buffer

*NuPAGE Tris-Acetate gels: For Native electrophoresis, use Invitrogen Tris-Glycine Native Running Buffer. For Denaturing electrophoresis, use NuPAGE Tris-Acetate SDS Running Buffer

*NuPAGE Bis-Tris gels: For Denaturing electrophoresis, use NuPAGE MOPS-SDS Running Buffer or NuPAGE MES-SDS Running Buffer

*Bolt Bis-Tris Plus gels: For Denaturing electrophoresis, use Bolt MOPS SDS Running Buffer or Bolt MES SDS Running Buffer

*Thermo Scientific Precise Tris-Glycine gels: For Native electrophoresis, use Tris-Glycine SDS Running Buffer without SDS added. For Denaturing electrophoresis, use Tris-Glycine SDS Running Buffer.

*Thermo Scientific Precise Tris-HEPES gels: For Denaturing electrophoresis, use Tris-HEPES SDS Running Buffer.

Find additional tips, troubleshooting help, and resources within our Protein Electrophoresis and Western Blotting Support Center.